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Masitinib in Patients With Mastocytosis With Handicap and Bearing the D816V Mutation

Primary Purpose

Mastocytosis

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
masitinib
Sponsored by
AB Science
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mastocytosis focused on measuring mastocytosis, D816V, handicaps

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with one of the following documented mastocytosis:

    • Smouldering systemic mastocytosis
    • Indolent systemic mastocytosis with organomegaly
    • Indolent Systemic Mastocytosis having 2 infiltrated organs (skin and bone-marrow)
    • Any mastocytosis with in the last 6 months at least 3 anaphylactic shocks or syncops requiring either use of adrenaline or medical assistance
    • Cutaneous Mastocytosis (CM)
  2. Skin biopsy-documented mastocytosis and evaluable disease based upon:

    • Histological criteria: typical infiltrates of mast cells in a multifocal or diffuse pattern in skin biopsy
    • Clinical criteria: typical skin lesions (maculopapular, urticaria pigmentosa, mastocytoma)
  3. Missing data (c-kit molecular analysis not done) or documented presence of an activating point mutation in the phosphotransferase domain of c-kit such as D816V c-kit mutation in at least one infiltrated organ (bone marrow or skin)
  4. Refractory to at least one of the symptomatic treatments such as:

    • Anti H1
    • Anti H2
    • Proton pump inhibitor
    • Osteoclast inhibitor
    • Cromoglycate Sodium
    • Antileukotriene
    • Other therapies used for the symptomatic care
  5. Handicap defined as at least one of the following handicaps:

    • pruritus score ≥ 6
    • number of flushes per week ≥ 7
    • number of stools per day ≥ 4 ,
    • number of mictions per day ≥ 8 ,
    • QLQ-C30 score ≥ 60,
    • Hamilton score ≥ 10

Exclusion Criteria:

  1. Patients with one of the following mastocytosis:

    • Systemic Mastocytosis with an Associated clonal Hematologic Non Mast cell lineage Disease (SM-AHNMD)
    • Mast cell leukemia (MCL)
    • Aggressive systemic mastocytosis (ASM)
  2. Patient with a major surgery within 2 weeks prior to study entry
  3. No vulnerable population will be included in this study

    • Life expectancy < 6 months.
    • Patient is < 5 years free of malignancy, except treated basal cell skin cancer or cervical carcinoma in situ.
    • Patient with grade III/IV cardiac problems as defined by the New York Heart Association Criteria. (i.e., congestive heart failure, myocardial infarction within 6 months of study)
    • Patient has a severe and/or uncontrolled medical disease.
    • Patient has a known diagnosis of human immunodeficiency virus (HIV) infection

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    masitinib 3 mg/kg/day

    masitinib 6 mg/kg/day

    Arm Description

    masitinib 3 mg/kg/day

    masitinib 6 mg/kg/day

    Outcomes

    Primary Outcome Measures

    efficacy on handicaps
    Pruritus score at week 12 Number of flushes per week at week 12 Hamilton score at week 12 Fatigue Impact scale at week 12

    Secondary Outcome Measures

    Full Information

    First Posted
    December 23, 2010
    Last Updated
    December 6, 2018
    Sponsor
    AB Science
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01266369
    Brief Title
    Masitinib in Patients With Mastocytosis With Handicap and Bearing the D816V Mutation
    Official Title
    A 12-week With Possible Extension, Prospective, Multicenter, Randomized, Open-label, 2-parallel Group, Phase IIa Study to Compare Efficacy and Safety of AB1010 at 3 or 6 mg/kg/Day in Treatment of Patients With Mastocytosis With Handicap and Bearing Activating Point Mutations in the Phosphotransferase Domain of c-Kit Such as the Main Mutation Asp-816-Val (D816V)
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2018
    Overall Recruitment Status
    Completed
    Study Start Date
    February 2007 (undefined)
    Primary Completion Date
    November 2007 (Actual)
    Study Completion Date
    May 2010 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    AB Science

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The objective is to compare efficacy and safety of AB1010 at 3 or 6 mg/kg/day in treatment of patients with mastocytosis with handicap and bearing activating point mutations in the phosphotransferase domain of c-Kit such as the main mutation Asp-816-Val (D816V).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Mastocytosis
    Keywords
    mastocytosis, D816V, handicaps

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    21 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    masitinib 3 mg/kg/day
    Arm Type
    Experimental
    Arm Description
    masitinib 3 mg/kg/day
    Arm Title
    masitinib 6 mg/kg/day
    Arm Type
    Experimental
    Arm Description
    masitinib 6 mg/kg/day
    Intervention Type
    Drug
    Intervention Name(s)
    masitinib
    Primary Outcome Measure Information:
    Title
    efficacy on handicaps
    Description
    Pruritus score at week 12 Number of flushes per week at week 12 Hamilton score at week 12 Fatigue Impact scale at week 12
    Time Frame
    week 12

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients with one of the following documented mastocytosis: Smouldering systemic mastocytosis Indolent systemic mastocytosis with organomegaly Indolent Systemic Mastocytosis having 2 infiltrated organs (skin and bone-marrow) Any mastocytosis with in the last 6 months at least 3 anaphylactic shocks or syncops requiring either use of adrenaline or medical assistance Cutaneous Mastocytosis (CM) Skin biopsy-documented mastocytosis and evaluable disease based upon: Histological criteria: typical infiltrates of mast cells in a multifocal or diffuse pattern in skin biopsy Clinical criteria: typical skin lesions (maculopapular, urticaria pigmentosa, mastocytoma) Missing data (c-kit molecular analysis not done) or documented presence of an activating point mutation in the phosphotransferase domain of c-kit such as D816V c-kit mutation in at least one infiltrated organ (bone marrow or skin) Refractory to at least one of the symptomatic treatments such as: Anti H1 Anti H2 Proton pump inhibitor Osteoclast inhibitor Cromoglycate Sodium Antileukotriene Other therapies used for the symptomatic care Handicap defined as at least one of the following handicaps: pruritus score ≥ 6 number of flushes per week ≥ 7 number of stools per day ≥ 4 , number of mictions per day ≥ 8 , QLQ-C30 score ≥ 60, Hamilton score ≥ 10 Exclusion Criteria: Patients with one of the following mastocytosis: Systemic Mastocytosis with an Associated clonal Hematologic Non Mast cell lineage Disease (SM-AHNMD) Mast cell leukemia (MCL) Aggressive systemic mastocytosis (ASM) Patient with a major surgery within 2 weeks prior to study entry No vulnerable population will be included in this study Life expectancy < 6 months. Patient is < 5 years free of malignancy, except treated basal cell skin cancer or cervical carcinoma in situ. Patient with grade III/IV cardiac problems as defined by the New York Heart Association Criteria. (i.e., congestive heart failure, myocardial infarction within 6 months of study) Patient has a severe and/or uncontrolled medical disease. Patient has a known diagnosis of human immunodeficiency virus (HIV) infection
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Olivier Lortholary, MD, PhD
    Organizational Affiliation
    Necker Hospital, Paris, France
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Masitinib in Patients With Mastocytosis With Handicap and Bearing the D816V Mutation

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